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Effect of crystalline Si3N4 fillers on the mechanical strength and thermal stability of complex SiCN(O) ceramic architectures produced by powder bed fusion and densified via polymer infiltration and pyrolysis 结晶Si3N4填料对粉末床熔合、聚合物渗透和热解致密复合SiCN(O)陶瓷结构机械强度和热稳定性的影响
IF 2.8 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-09-13 DOI: 10.1016/j.oceram.2025.100846
Marco Pelanconi , Samuele Bottacin , Mario Caccia , Alberto Ortona , Yawei Li
Silicon nitride is a high-performance ceramic recognized for its mechanical, thermal, and chemical stability at elevated temperatures. In this study, we present a novel method to fabricate macroporous Si₃N₄ ceramics via powder bed fusion of polyamide mixed with 0-40 vol% of crystalline Si₃N₄ powder. The printed preforms were subsequently infiltrated with a polysilazane polymer and pyrolyzed to form SiCN(O) matrices containing β-Si₃N₄ particles. A rotated cube lattice was selected as a benchmark geometry and scaled to compensate for shrinkage. The effects of ceramic filler content on densification, microstructure, strength, and oxidation resistance at 1500 °C were investigated. Increasing β-Si₃N₄ content improved the relative density, compressive strength, and thermal stability of the final ceramics. Particularly, 20–40 vol% Si₃N₄ enhanced oxidation resistance by forming a protective silica-rich surface layer and stabilizing the underlying structure. This study highlights an effective strategy to tailor the high-temperature behaviour of polymer-derived ceramics for advanced structural applications.
氮化硅是一种高性能陶瓷,因其在高温下的机械、热和化学稳定性而得到认可。在这项研究中,我们提出了一种新的方法,通过将聚酰胺与0-40体积%的结晶Si₃N₄粉末混合的粉末床熔融来制备大孔Si₃N₄陶瓷。随后,用聚硅氮烷聚合物浸润打印的预成型物,并热解形成含有β-Si₃N₄颗粒的SiCN(O)基质。选择旋转的立方体晶格作为基准几何,并缩放以补偿收缩。研究了填料含量对合金致密化、显微组织、强度和1500℃抗氧化性能的影响。增加β-Si₃N₄的含量,提高了陶瓷的相对密度、抗压强度和热稳定性。特别是,20-40 vol% Si₃N₄通过形成保护性的富硅表面层和稳定底层结构来增强抗氧化性。这项研究强调了一种有效的策略来定制聚合物衍生陶瓷的高温行为,用于先进的结构应用。
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引用次数: 0
Microstructure and adsorption studies on the simultaneous removal of Cu2+, Ni2+, and Zn2+ from simulated wastewater using magnetically functionalized Philippine natural zeolite composite 磁性功能化菲律宾天然沸石复合材料同时去除模拟废水中Cu2+、Ni2+和Zn2+的微观结构和吸附研究
IF 2.8 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-09-09 DOI: 10.1016/j.oceram.2025.100845
Belinda B. Faustino , Reynaldo M. Vequizo , Rolando T. Candidato Jr.
This study reports the microstructural characteristics and adsorption properties for heavy metal ions of the surface-modified Philippine natural zeolite (MPNZ) and magnetically functionalized Philippine natural zeolite (PNZM) composite. SEM analysis confirmed the presence of magnetite particles dispersed on PNZM, making its surface rougher and irregular while retaining its porous structure. X-ray diffractogram revealed distinct peaks corresponding to the spinel crystalline structure of magnetite and the aluminosilicate structure of the zeolite framework, suggesting a well-integrated composite material. BET analysis showed an increase in the surface area of MPNZ from 33.876 m2/g to 45.052 m2/g after adding magnetite. EDS characterization verified the strong presence of Fe+ ions in the PNZM structure, enhancing its cation-exchange capacity (CEC). The Si/Al ratio of MPNZ decreased from 3.75 to 3.37, indicating a more negative charge, supported by zeta potential results that showed surface charges of (-)12.200 for MPNZ to (-) 20.854 mV for PNZM. In single ion solutions, PNZM obtained a removal uptake of 98.85 %, 99.99 % and 99.48 % for Ni2+, Cu2+and Zn2+ respectively, which are higher than MPNZ. In mixed-ion solutions, PNZM also showed improved adsorption with removal rates of 91.17 % for Ni2+ and 97.90 % for Cu2+, although Zn2+ uptake decreased to 97.98 % compared to the 99.99 % of MPNZ. Overall, incorporating magnetite has functionalized the ability of PNZM for sustainable water treatment by removing heavy metal ions through the synergistic mechanism of ion-exchange and Coulombic electrostatic interactions.
研究了表面改性菲律宾天然沸石(MPNZ)和磁功能化菲律宾天然沸石(PNZM)复合材料的微观结构特征和对重金属离子的吸附性能。SEM分析证实,PNZM表面存在分散的磁铁矿颗粒,使其表面更加粗糙和不规则,同时保留了其多孔结构。x射线衍射图显示磁铁矿尖晶石晶体结构和沸石骨架铝硅酸盐结构相对应的明显峰,表明复合材料具有良好的整体性。BET分析表明,加入磁铁矿后,MPNZ的比表面积由33.876 m2/g增加到45.052 m2/g。EDS表征证实了PNZM结构中Fe+离子的存在,增强了其阳离子交换能力(CEC)。MPNZ的Si/Al比值从3.75下降到3.37,表明MPNZ具有更多的负电荷,zeta电位结果表明MPNZ的表面电荷为(-)12.200 mV, PNZM的表面电荷为(-)20.854 mV。在单离子溶液中,PNZM对Ni2+、Cu2+和Zn2+的去除率分别为98.85%、99.99%和99.48%,均高于MPNZ。在混合离子溶液中,PNZM对Ni2+的去除率为91.17%,对Cu2+的去除率为97.90%,而Zn2+的去除率为97.98%,而MPNZ的去除率为99.99%。总的来说,加入磁铁矿使PNZM通过离子交换和库仑静电相互作用的协同机制去除重金属离子,从而功能化了PNZM可持续水处理的能力。
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引用次数: 0
The study of natural dolomite as a prospective material for CO2 capture employing a novel approach to the evaluation of breakthrough curves 采用一种新的方法来评估突破曲线,研究天然白云岩作为二氧化碳捕获的有前景的材料
IF 2.8 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-09-09 DOI: 10.1016/j.oceram.2025.100844
Anna Imrichová , Patrik Sokola , Jiří Másilko , Marek Baláš , Vladislav Cába , Kateřina Karásková , Jiří Švec , Petr Ptáček
The capture of carbon dioxide (CO2) is a critical technology for addressing climate change and sustainability objectives. In this study, the performance of natural dolomite as an effective sorbent for repeated CO2 capture was evaluated. The results suggested that an optimal calcination temperature of 850 °C was beneficial for minimizing surface sintering of the dolomite, thereby facilitating effective decarbonation. Breakthrough curve analysis was conducted to evaluate the dynamic adsorption performance of dolomite at varying CO2 concentrations (10 %, 12 %, and 16 %). To assess the progress of gas adsorption onto regenerated dolomite, an innovative method of curve fitting using the modified Avrami equation was employed, which provided three essential parameters for the adsorption process: retention time, rate constant, and Avrami coefficient. A steady decrease in breakthrough time and adsorption efficiency was found to be correlated with sintering and surface area loss. The maximum CO2 adsorption capacity was achieved during the second or third cycle for all three measured CO2 concentrations; however, performance gradually deteriorated in subsequent cycles due to surface sintering and a reduction in specific surface area. TPD and BET analyses supported the conclusion that the surface area decreased with repeated regeneration, and the basic active sites were reduced.
二氧化碳捕集是应对气候变化和实现可持续发展目标的关键技术。在这项研究中,天然白云石作为一种有效的吸附剂,反复捕获二氧化碳的性能进行了评估。结果表明,850℃的最佳焙烧温度有利于减少白云石的表面烧结,从而促进有效的脱碳。通过突破曲线分析,评价了不同CO2浓度(10%、12%和16%)下白云石的动态吸附性能。为了评估再生白云岩上气体吸附的进展,采用了一种基于修正Avrami方程的创新曲线拟合方法,该方法提供了吸附过程的三个基本参数:保留时间、速率常数和Avrami系数。突破时间和吸附效率的稳定下降与烧结和表面积损失有关。在第二次或第三次循环中,所有三种测量的CO2浓度均达到最大CO2吸附量;然而,在随后的循环中,由于表面烧结和比表面积的减少,性能逐渐恶化。TPD和BET分析表明,随着再生的不断进行,其表面积减小,基本活性位点减少。
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引用次数: 0
Synthesis and characterization of LLZNO & LLZTO: Insights into the impact of different lithium precursors on properties LLZNO和LLZTO的合成与表征:不同锂前驱体对性能的影响
IF 2.8 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-09-03 DOI: 10.1016/j.oceram.2025.100842
Chengjian Li , Frank Kern , Lianmeng Liu , Christopher Parr , Andreas Börger , Chunfeng Liu
Garnet-type Li₇La₃Zr₂O₁₂ (LLZO) is a promising solid electrolyte for all-solid-state batteries due to its high ionic conductivity and excellent thermal stability. However, production of high performance LLZO remains constrained by the reliance on high-purity reagents and complex synthesis routes. This study presents a cost-effective strategy to prepare high-performance Ta- and Nb-doped LLZO using commercially sourced raw materials via conventional solid-state reaction. Two lithium precursors, Li2CO3 and LiOH·H₂O, were systematically compared to evaluate their impacts on formation and performances of LLZO. LiOH-derived powders showed higher phase purity and finer morphology, while Li2CO3-derived powders offered better processability. While the LLZNO-LOH sample achieved 94.4% relative density and 0.78 × 10⁻3 S/cm conductivity, LLZTO-LCO also reached 0.75 × 10⁻3 S/cm with a relative density of 94.1%. All sintered samples exhibited phase-pure cubic garnet structures. These findings demonstrate the industrial feasibility of LLZO production, paving the way for its practical deployment in next-generation solid-state batteries.
garnet型Li₇La₃Zr₂O₁₂(LLZO)是一种很有前途的全固态电池固体电解质,因为它具有高离子电导率和优异的热稳定性。然而,高性能LLZO的生产仍然受到高纯度试剂和复杂合成路线的限制。本研究提出了一种具有成本效益的策略,利用商业来源的原料,通过传统的固态反应制备高性能的掺杂Ta和nb的LLZO。系统比较了两种锂前驱体Li2CO3和LiOH·H₂O对LLZO形成和性能的影响。lioh衍生粉末具有较高的相纯度和较细的形貌,而li2co3衍生粉末具有较好的加工性能。llzo - loh样品的相对密度为94.4%,电导率为0.78 × 10秒/厘米,LLZTO-LCO样品的相对密度为94.1%,也达到0.75 × 10秒/厘米。所有烧结样品均呈现相纯立方石榴石结构。这些发现证明了LLZO生产的工业可行性,为其在下一代固态电池中的实际应用铺平了道路。
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引用次数: 0
Temperature effects of defect formation in BeO ceramics during helium blistering 氦泡胀过程中BeO陶瓷缺陷形成的温度效应
IF 2.8 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-09-01 DOI: 10.1016/j.oceram.2025.100843
Azamat E. Ryskulov , Artem L. Kozlovskiy , Igor A. Ivanov , Inesh E. Kenzhina , Marina Konuhova
The work is devoted to the study of the processes of defect accumulation in the near-surface layer of BeO ceramics associated with irradiation with low-energy He2+ ions, as well as to the establishment of the role of temperature effects on changes in thermal conductivity. Identification of the role of temperature effects in acceleration of the processes of distortion and disordering of the near-surface layers is one of the key tasks, the solution of which will allow more accurate prediction of the behavior of materials under extreme conditions combining the effects of high temperatures and radiation damage. During assessment of changes in structural parameters depending on variations in irradiation conditions, anisotropic distortion of the crystal lattice, the degree of deformation of which has a direct relationship with the temperature effect, was established. It has been determined that an increase in the irradiation temperature leads to an acceleration of the processes of accumulation of deformation distortions, the growth of which in the damaged layer leads to a more pronounced destabilization and broadening of the damaged layer depth. Such changes are associated with the acceleration of the diffusion processes of point and vacancy defects, the migration of which leads not only to an increase in deformation distortions and amorphous inclusions, but also to an increase in the damaged layer thickness. During determination of changes in the concentration of vacancy and structural defects in the damaged layer, relationships between the concentration of oxygen vacancies and the degradation of thermal conductivity, the reduction of which is due to an increase in the effects of phonon scattering and a decrease in the rate of heat transfer, were established.
本工作致力于研究低能He2+离子辐照下BeO陶瓷近表层缺陷积累的过程,以及建立温度效应对导热系数变化的作用。确定温度效应在加速近表层变形和无序过程中的作用是关键任务之一,解决这一问题将允许更准确地预测材料在极端条件下的行为,结合高温和辐射损伤的影响。在评估结构参数随辐照条件变化的变化时,建立了晶格的各向异性畸变,其变形程度与温度效应有直接关系。已经确定,辐照温度的升高导致变形变形积累过程的加速,变形变形在损伤层中的增长导致更明显的不稳定和损伤层深度的扩大。这种变化与点缺陷和空位缺陷扩散过程的加速有关,点缺陷和空位缺陷的迁移不仅导致变形变形和非晶夹杂的增加,而且导致损伤层厚度的增加。在测定损伤层中空位和结构缺陷浓度的变化过程中,建立了氧空位浓度与导热系数下降之间的关系,导热系数的降低是由于声子散射效应的增加和传热速率的降低。
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引用次数: 0
Determination of the prospects for the use of multicomponent composite ceramics as thermal barrier protective coatings 多组分复合陶瓷热障防护涂层应用前景的确定
IF 2.8 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-09-01 DOI: 10.1016/j.oceram.2025.100838
Ye.A. Kenzhin , D.I. Shlimas , A.M. Zikirina , A.L. Kozlovskiy
The paper presents the results of experiments aimed at identification of the influence of variations in thermal sintering conditions on the phase transformation processes in multicomponent ceramics based on oxide compounds of cerium, tellurium, bismuth, tungsten and zinc. According to the data obtained, it was established that with the annealing temperature growth above 1000 °C, the observed growth of zinc tungstate inclusions is due to the processes of recrystallization of the ZnTeO3 and Bi₂WO₆ phases, which lead to the growth of grains of the ZnWO4 phase and the formation of glass-like inclusions that have a reinforcing effect. During the studies conducted it was determined that the formation of inclusions in the form of zinc tungstate in the composition of multicomponent ceramics, caused by the thermal effect of sintering, leads to an increase in the resistance of ceramics to external influences, and also enhances resistance to high-temperature destruction and hydrogenation processes. An analysis of the thermal insulation characteristics of the studied ceramics showed that the dominance of zinc tungstate inclusions in the composition of the ceramics leads to increased resistance to both the processes of destruction caused by hydrogenation and thermal aging, the long-term impact of which leads to increased destabilization of the strength properties of the ceramics and deterioration of thermal insulation.
本文介绍了热烧结条件变化对铈、碲、铋、钨和锌氧化物复合材料多组分陶瓷相变过程影响的实验结果。根据所得数据确定,在退火温度高于1000℃时,观察到的钨酸锌夹杂物的生长是由于ZnTeO3相和Bi₂WO₆相的再结晶过程,导致ZnWO4相晶粒长大,形成具有增强作用的玻璃状夹杂物。在进行的研究中,确定了在多组分陶瓷的组成中,由于烧结的热效应而形成的钨酸锌形式的夹杂物,导致陶瓷对外界影响的抵抗力增加,同时也增强了对高温破坏和氢化过程的抵抗力。对所研究陶瓷的保温特性分析表明,钨酸锌夹杂物在陶瓷成分中占主导地位,导致陶瓷对氢化破坏和热老化过程的抵抗能力增强,长期的氢化破坏和热老化的影响导致陶瓷强度性能的不稳定性增加,保温性能恶化。
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引用次数: 0
Structural and microstructural evolution of fused filament fabricated SiOC(N) via polymer-derived ceramics route 聚合物衍生陶瓷熔丝制备SiOC(N)的结构与微观结构演变
IF 2.8 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-09-01 DOI: 10.1016/j.oceram.2025.100839
Rajat Chaudhary , Jonathan Selorm Degbedzui , Mattia Biesuz , Gian Domenico Sorarù
Cellular SiOC(N) ceramics were produced by impregnating a 3D-printed TPU lattice with polysilazane, followed by pyrolysis in an inert atmosphere. During pyrolysis, TPU decomposes while polysilazane converts to ceramic. The process was analyzed across the full temperature range via weight loss, shrinkage, density, porosity, specific surface area, FTIR and Vickers hardness.
TPU decomposes between 380 and 550 °C with significant weight loss, while ceramization of polysilazane occurs between 550 and 800 °C, forming SiOC(N). Transient micro- and mesoporosity develops only at 600–700 °C. Skeletal density and hardness increase steadily up to 1200 °C.
通过在3d打印的TPU晶格中浸渍聚硅氮烷,然后在惰性气氛中热解,制备了多孔SiOC(N)陶瓷。在热解过程中,TPU分解,聚硅氮烷转化为陶瓷。在整个温度范围内,通过失重、收缩率、密度、孔隙率、比表面积、红外光谱和维氏硬度对该过程进行了分析。TPU在380 ~ 550℃之间分解,重量损失显著,而聚硅氮烷在550 ~ 800℃之间发生陶化,形成SiOC(N)。瞬态微孔和介孔仅在600-700°C时发生。骨骼密度和硬度稳定增加到1200°C。
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引用次数: 0
Use of ladle furnace slag as filler replacement in magnesium oxychloride cement: Towards sustainable 3D-printable building composites 使用钢包炉渣作为氯氧镁水泥的填料替代品:走向可持续的3d打印建筑复合材料
IF 2.8 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-09-01 DOI: 10.1016/j.oceram.2025.100841
Ondřej Jankovský , Petr Lodňánek , Anna-Marie Lauermannová , Adéla Jiříčková , Jozef Vlček , Hana Ovčačíková , Michaela Topinková , Petra Maierová , Jiří Fiedor , Petr Miarka , Martina Záleská , Adam Pivák , Milena Pavlíková , Zbyšek Pavlík
In response to the global demand for CO2 emissions reduction, Portland cement (PC) replacement with more eco-friendly materials has been focused on in material studies. One of the studied alternatives is magnesium oxychloride cement (MOC), which offers excellent mechanical properties and lower production temperatures. The ecological impact of MOC alone is significant, but if we incorporate waste material as a filler replacement in MOC composites, we can decrease overall emissions even more. In this paper, we focused on the development of an eco-friendly material with a safely incorporated ladle furnace slag (SL). Firstly, the SL was characterized by numerous analytical methods (XRF, XRD, SEM, EDS, STA-MS) to attain knowledge about its elemental and phase composition. In the following step, MOC composite materials with SL used as a silica sand partial replacement were prepared by casting. Such prepared materials were then characterized by XRF, XRD, SEM, EDS, and MIP. Furthermore, their structural and mechanical properties were assessed. Based on the obtained results, an optimized composition of mixtures was used for 3D printing to demonstrate the suitability of this material for this purpose. Finally, X-ray computed micro-tomography imaging was used to study the quality of printed cubes, in particular porosity and the amount of macroscopic defects. This paper presents an innovative approach in which waste SL from steel production can replace silica sand filler in significant quantities, demonstrating that such a designed material is suitable for additive manufacturing.
为了响应全球对二氧化碳减排的需求,用更环保的材料替代波特兰水泥(PC)一直是材料研究的重点。研究的替代品之一是氯氧镁水泥(MOC),它具有优异的机械性能和较低的生产温度。MOC本身的生态影响是显著的,但如果我们将废物作为MOC复合材料的填料替代品,我们可以减少总体排放更多。在本文中,我们专注于开发一种安全掺入钢包炉渣(SL)的环保材料。首先,通过多种分析方法(XRF, XRD, SEM, EDS, STA-MS)对SL进行了表征,以了解其元素和相组成。在接下来的步骤中,采用铸造法制备了以SL作为硅砂部分替代品的MOC复合材料。然后用XRF, XRD, SEM, EDS和MIP对所制备的材料进行了表征。并对其结构和力学性能进行了评价。基于所获得的结果,优化的混合物组合用于3D打印,以证明该材料用于此目的的适用性。最后,利用x射线计算机微断层成像技术研究了打印立方体的质量,特别是孔隙率和宏观缺陷的数量。本文提出了一种创新的方法,在这种方法中,钢铁生产中的废料SL可以大量替代硅砂填料,这表明这种设计的材料适用于增材制造。
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引用次数: 0
Structural, optical, and magnetic properties of sol-gel method synthesized Zn0.5NixCo0.5-xFe2O4 nanoferrites 溶胶-凝胶法合成Zn0.5NixCo0.5-xFe2O4纳米铁氧体的结构、光学和磁性能
IF 2.8 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-08-29 DOI: 10.1016/j.oceram.2025.100840
Abdien Y. Khalafallah , Mohamed A. Siddig , Abdullah Ahmed A Alghamdi , Obaidallah A. Algethami , Abdulraoof I.A. Ali , Rafat M. Ibrahim , Hassan H.E. Idris , Elsammani A. Shokralla
Structural, optical, and magnetic characteristics of ferrite compounds with formula of Zn0.5NixCo0.5-xFe2O4 (where x varies from 0.0 to 0.4) were prepared with the sol-gel synthesis method. Analysis using X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy indicated cubic spinel structure. Notably, the crystallite size showed to be decreased from 60.25 nm to 15.85 nm as Ni content increased, accompanied by enhancements of both volume and density. Optical assessments using UV–visible spectroscopy demonstrated reduction in absorbance values from 1.01 a.u. to 0.32 a.u. A slight increase observed in the energy band gap from 5.664 to 5.684 eV with increasing Ni substitution. The magnetic properties were influenced by the replacement of Ni+2 with Co+2 exhibiting superparamagnetic behavior, with coercivity values ranging from 26.422 to 126.680 Oe and saturation magnetization peaking at x = 0.2 (33.239 emu/g). The magnetic behavior suggests that the Ni-doped nanoparticles are promising materials for applications in sensing, soft magnets, and hyperthermia treatments.
采用溶胶-凝胶合成方法制备了分子式为Zn0.5NixCo0.5-xFe2O4 (x为0.0 ~ 0.4)的铁氧体化合物的结构、光学和磁性特征。x射线衍射(XRD)和傅里叶变换红外光谱(FTIR)分析表明,尖晶石结构为立方结构。值得注意的是,随着Ni含量的增加,晶粒尺寸从60.25 nm减小到15.85 nm,体积和密度都有所增加。紫外-可见光谱的光学评估表明,吸光度值从1.01 a.u.降低到0.32 a.u.。随着Ni取代量的增加,能带隙从5.664 eV略微增加到5.684 eV。Ni+2被Co+2取代后,其磁性能呈现出超顺磁性,矫顽力值在26.422 ~ 126.680 Oe之间,饱和磁化强度在x = 0.2 (33.239 emu/g)处达到峰值。磁性行为表明,镍掺杂纳米颗粒在传感、软磁体和热疗方面的应用前景广阔。
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引用次数: 0
Thermal cycling of YAG infiltration and plasma sprayed coatings as environmental barrier coating on ceramic heat shields for use in hydrogen operating gas turbines 用于氢气燃气轮机的陶瓷隔热板的YAG渗透和等离子喷涂涂层作为环境屏障涂层的热循环
IF 2.8 Q1 MATERIALS SCIENCE, CERAMICS Pub Date : 2025-08-18 DOI: 10.1016/j.oceram.2025.100837
J.C. Müller-Elmau , A. Göbel , P. Junge , J.T. Müller , T.C. Rousseau , O. Görke , C. Nikasch , S. Kiliani
Environmental barrier coatings (EBC) are intended to protect alumina ceramic tiles in hot water vapor conditions, enabling gas turbines to operate with higher hydrogen content or even pure hydrogen. For these operating conditions, yttrium aluminum garnet (YAG) promises the highest protection against hydrolysis, which can be applied via atmospheric plasmaspraying (APS). To enhance the protection efficiency, the coating is combined with a prior infiltration of the base material. The obtained design acts as in-depth protection even if the coating exhibits cracks.
环境屏障涂层(EBC)旨在保护热水蒸气条件下的氧化铝瓷砖,使燃气轮机能够在高氢含量甚至纯氢的情况下运行。对于这些操作条件,钇铝石榴石(YAG)承诺最高的防水解保护,可通过大气等离子体喷涂(APS)应用。为了提高保护效率,涂层与基材的预先渗透相结合。即使涂层出现裂缝,所获得的设计也可以起到深度保护的作用。
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引用次数: 0
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Open Ceramics
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